BEUDAMED
    FDA Adverse Event Other Summary report: N

    LATEX EXAM GLOVES

    MDR report key: 208467 · Received February 3, 1999

    Report

    Report Number
    1423507-1999-00021
    Event Type
    Other
    Date Received
    February 3, 1999
    Date of Event
    January 11, 1999
    Report Date
    February 3, 1999
    Manufacturer
    ALLEGIANCE HEALTHCARE CORP.
    Product Code
    LYY
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IL, US
    Reporter Occupation
    ATTORNEY

    Narratives

    Description of Event or Problem · 1

    PLAINTIFF ALLEGES DEVELOPING A SEVERE ALLERGY TO LATEX GLOVES FROM WEARING THE LATEX GLOVES AND AS A RESULT HAS EXPERIENCE ALLERGIC REACTIONS TO LATEX PRODUCTS AND IS UNABLE TO BE IN HER WORK INVIRONMENT DUE TO THE PRESENCE OF LATEX PRODUCTS. FURTHER ALLEGES THAT SHE HAS BEEN SEVERELY DAMAGED IN HER ABILITY TO PARTICIPATE IN THE AFFAIRS OF LIFE AND HER EARNINGS CAPABILITY AND HAS LOST EARNINGS THAT WOULD HAVE OCCURRED TO HER, AND INCURRED MEDICAL BILLS IN ATTEMPTING TO DIAGNOSE AND TREAT HER CONDITION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LATEX EXAM GLOVES LATEX EXAM GLOVES LYY ALLEGIANCE HEALTHCARE CORP. UNK UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other